Kimberly and Eric J. Waldman Department of Dermatology, Mark Lebwohl Center for Neuroinflammation and Sensation, Marc and Jennifer Lipschultz Precision Immunology Institute, and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Center for Substance Abuse Research, Lewis Katz School of Medicine, Temple University, Philadelphia, Pennsylvania, USA.
Exp Dermatol. 2022 Dec;31(12):1900-1907. doi: 10.1111/exd.14669. Epub 2022 Sep 23.
Modern genetic approaches in animal models have unveiled novel itch-specific neural pathways, emboldening a paradigm in which drugs can be developed to selectively and potently target itch in a variety of chronic pruritic conditions. In recent years, kappa-opioid receptors (KORs) and mu-opioid receptors (MORs) have been implicated in both the suppression and promotion of itch, respectively, by acting on both the peripheral and central nervous systems. The precise mechanisms by which agents that modulate these pathways alleviate itch remains an active area of investigation. Notwithstanding this, a number of agents have demonstrated efficacy in clinical trials that influence both KOR and MOR signalling. Herein, we summarize a number of opioid receptor modulators in development and their promising efficacy across a number of chronic pruritic conditions, such as atopic dermatitis, uremic pruritus and beyond.
现代遗传方法在动物模型中揭示了新的瘙痒特异性神经通路,这为开发药物以选择性和有效地针对各种慢性瘙痒疾病中的瘙痒提供了范例。近年来,κ-阿片受体(KOR)和μ-阿片受体(MOR)分别通过作用于外周和中枢神经系统,分别被认为与瘙痒的抑制和促进有关。调节这些途径的药物减轻瘙痒的确切机制仍然是一个活跃的研究领域。尽管如此,许多已证明在影响 KOR 和 MOR 信号的临床试验中有效的药物。在此,我们总结了一些正在开发中的阿片受体调节剂及其在多种慢性瘙痒疾病中的有希望的疗效,如特应性皮炎、尿毒症瘙痒等。